Hydroquinone

Hydroquinone

SCHEMBL9777901

O=C(c1ccc(Cl)cc1)c1ccc(Cl)cc1.Oc1ccc(O)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPK1 P28482 1/20 1.00
HPGD P15428 2/20 0.75
LMNA P02545 2/20 0.75
MAPT P10636 2/20 0.75
ESR1 P03372 2/20 0.75
ESR2 Q92731 2/20 0.75
PKM P14618 1/20 0.75
HTT P42858 1/20 0.75
SRD5A2 P31213 2/20 0.67
RAB9A P51151 2/20 0.59
NPC1 O15118 1/20 0.59
CES2 O00748 1/20 0.56
CES1 P23141 1/20 0.56
MEN1 O00255 1/20 0.56
KMT2A Q03164 1/20 0.56
CXCL12 P48061 1/20 0.55
CNR1 P21554 1/20 0.55
CNR2 P34972 1/20 0.55
MAOB P27338 1/20 0.55
ALOX15 P16050 1/20 0.54

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL9777896 1.00 MAPK1 (1.00) MAPK1HPGDLMNAMAPTESR1
SCHEMBL9457019 1.00 MAPK1 (1.00) MAPK1HPGDLMNAMAPTESR1
Hydroquinone SCHEMBL10635396 1.00 MAPK1 (1.00) MAPK1HPGDLMNAMAPTESR1
SCHEMBL333466 1.00 MAPK1 (1.00) MAPK1HPGDLMNAMAPTESR1
SCHEMBL29217821 0.98 MAPK1 (0.95) MAPK1HPGDLMNAMAPTESR1
Hydroquinone SCHEMBL9777898 0.98 MAPK1 (0.95) MAPK1HPGDLMNAMAPTESR1
SCHEMBL9777899 0.98 MAPK1 (0.95) MAPK1HPGDLMNAMAPTESR1
SCHEMBL30496095 0.98 MAPK1 (0.95) MAPK1HPGDLMNAMAPTESR1
SCHEMBL9248915 0.93 MAPK1 (0.87) MAPK1HPGDLMNAMAPTESR1
SCHEMBL2168586 0.93 MAPK1 (0.87) MAPK1HPGDLMNAMAPTESR1

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 1 patent. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5053477-A Reacting aromatic dihydroxy compound and aromatic dihalogeno compound containing a keto group in N-alkylcaprolactam solvent with mixture of alkali metal compounds including a carbonate BAYER AKTIENGESELLSCHAFT (DE) 1991-10-01 US disclosed